Sonication-induced J-aggregation in nonhalogenated solvents boosts exciton delocalization for high-efficiency organic solar cells

The commercialization of organic solar cells (OSCs) requires eliminating halogenated solvents. However, the disordered molecular aggregation of nonfullerene acceptors (NFAs) in nonhalogenated solvents hinders achieving high power conversion efficiencies (PCEs). Herein, this problem is addressed using an external physical field modulation strategy involving the sonication of NFA solutions to induce a transformation from disordered molecular aggregation to ordered J-aggregation via microstreaming and shear stress. The aggregation is effectively preserved within films, enhancing π-π stacking interactions. Moreover, sonication promotes the conversion of localized excitons to intra-moiety delocalized excitons and suppresses molecular vibrations. The PCEs of PM6:L8-BO-based binary and ternary devices fabricated using o-xylene are 19.43% and 20.41% (certified 19.84%), ranking among the highest values reported for nonhalogenated solvent-processed OSCs. The binary devices also exhibit high thermal stabilities (T<sub>80</sub> lifetime > 10000 h). This universally applicable strategy effectively controls disordered aggregation in NFA solutions, thus paving the way for practical industrial applications.

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Publication Details

Journal
Nature Communications
Published
2025-11-25
DOI
https://doi.org/10.1038/s41467-025-65447-y
Citations
3
Primary Topic
Organic Electronics and Photovoltaics
Type
article
Field-Weighted Citation Impact
2.19
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article

Sonication-induced J-aggregation in nonhalogenated solvents boosts exciton delocalization for high-efficiency organic solar cells

Xiaoyan Du, Wei Qin, Zhixiang Wei, Jiwei Cui et al.
3 citations
Nature Communications
Organic Electronics and Photovoltaics
2.19
article

Sonication-induced J-aggregation in nonhalogenated solvents boosts exciton delocalization for high-efficiency organic solar cells

Xiaoyan Du, Wei Qin, Zhixiang Wei, Jiwei Cui, Muthupandian Ashokkumar, Ruyue Zhang, Kun Gao, Trevor A. Smith, Jiawei Qiao, Yue Wu, Xiaotao Hao, Christopher R. Hall, Hang Yin, Yanming Sun, Feng Chen, Tong Wang, Dongrui Wang, Kangning Zhang, Jiali Song, Xinyue Xu, Mingxu Zhou
article en
3 citations

Abstract

The commercialization of organic solar cells (OSCs) requires eliminating halogenated solvents. However, the disordered molecular aggregation of nonfullerene acceptors (NFAs) in nonhalogenated solvents hinders achieving high power conversion efficiencies (PCEs). Herein, this problem is addressed using an external physical field modulation strategy involving the sonication of NFA solutions to induce a transformation from disordered molecular aggregation to ordered J-aggregation via microstreaming and shear stress. The aggregation is effectively preserved within films, enhancing π-π stacking interactions. Moreover, sonication promotes the conversion of localized excitons to intra-moiety delocalized excitons and suppresses molecular vibrations. The PCEs of PM6:L8-BO-based binary and ternary devices fabricated using o-xylene are 19.43% and 20.41% (certified 19.84%), ranking among the highest values reported for nonhalogenated solvent-processed OSCs. The binary devices also exhibit high thermal stabilities (T<sub>80</sub> lifetime > 10000 h). This universally applicable strategy effectively controls disordered aggregation in NFA solutions, thus paving the way for practical industrial applications.

Nature CommunicationsVol. 16(1)
Nanjing Agricultural University (CN), Shandong University (CN), The University of Melbourne (AU), National Center for Nanoscience and Technology (CN), Beihang University (CN)
Openalex Percentile: Top 11%
Organic Electronics and Photovoltaics
2.19
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